Department of Urology, Kidney Center, Tokyo Women's Medical University, 8-1 Kawada-cho, Shinjuku-ku, Tokyo, Japan, 162-8666.
Target Oncol. 2016 Oct;11(5):605-617. doi: 10.1007/s11523-016-0430-0.
Cancer cachexia is associated with patient outcomes.
The objective was to evaluate the effect of cachexia on survival among patients with metastatic renal cell carcinoma (mRCC) who had received first-line sunitinib treatment.
Seventy-one patients were retrospectively evaluated. Sarcopenia was diagnosed using sex-specific cut-offs for skeletal muscle index (measured using pre-treatment computed tomography) that were adjusted for body mass index. The modified Glasgow prognostic score (mGPS) was measured using C-reactive protein (CRP) and albumin levels (mGPS 2: CRP >1.0 mg/dL and albumin <3.5 g/dL; mGPS 1: CRP >1.0 mg/dL; mGPS 0: CRP ≤1.0 mg/dL). Progression-free survival (PFS) and overall survival (OS) were analyzed using the Kaplan-Meier method and Cox proportional hazard models.
Forty-five patients (63.4 %) had sarcopenia, with 53 (74.6 %), ten (14.1 %), and eight (11.3 %) patients having an mGPS of 0, 1, and 2, respectively. Sarcopenia was associated with significantly inferior PFS and OS, compared to non-sarcopenic patients (PFS: 7.6 vs. 18.2 months, p = 0.0004; OS: 22.3 months vs. not reached, p = 0.0019). Higher mGPS was associated with inferior PFS and OS (mGPS 0, 1, and 2: PFS = 11.5, 10.9, and 4.12 months, p < 0.0001; OS = 47.2, not reached, and 5.28 months, p < 0.0001; respectively). Sarcopenia was an independent predictor of shorter PFS (p = 0.0163), and mGPS was an independent predictor of shorter OS (p = 0.0012).
Sarcopenia and mGPS can predict outcomes among patients with mRCC who are receiving first-line sunitinib treatment.
癌症恶病质与患者预后相关。
本研究旨在评估恶病质对接受一线舒尼替尼治疗的转移性肾细胞癌(mRCC)患者生存的影响。
共回顾性评估了 71 例患者。采用针对特定性别的骨骼肌指数(通过治疗前 CT 测量,根据 BMI 进行调整)截断值诊断肌少症。改良格拉斯哥预后评分(mGPS)采用 C 反应蛋白(CRP)和白蛋白水平测量(mGPS2:CRP>1.0mg/dL 且白蛋白<3.5g/dL;mGPS1:CRP>1.0mg/dL;mGPS0:CRP≤1.0mg/dL)。采用 Kaplan-Meier 方法和 Cox 比例风险模型分析无进展生存期(PFS)和总生存期(OS)。
45 例(63.4%)患者存在肌少症,其中 53 例(74.6%)、10 例(14.1%)和 8 例(11.3%)患者的 mGPS 分别为 0、1 和 2。与非肌少症患者相比,肌少症患者的 PFS 和 OS 显著更差(PFS:7.6 个月 vs. 18.2 个月,p=0.0004;OS:22.3 个月 vs. 未达到,p=0.0019)。更高的 mGPS 与更差的 PFS 和 OS 相关(mGPS0、1 和 2:PFS=11.5、10.9 和 4.12 个月,p<0.0001;OS=47.2、未达到和 5.28 个月,p<0.0001;分别)。肌少症是 PFS 更短的独立预测因素(p=0.0163),mGPS 是 OS 更短的独立预测因素(p=0.0012)。
肌少症和 mGPS 可预测接受一线舒尼替尼治疗的 mRCC 患者的结局。